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rs17222919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17222919(G;G)
Make rs17222919(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position30734192
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs17222919
ebirs17222919
HLIrs17222919
Exacrs17222919
Varsomers17222919
Maprs17222919
PheGenIrs17222919
hapmaprs17222919
1000 genomesrs17222919
hgdprs17222919
ensemblrs17222919
gopubmedrs17222919
geneviewrs17222919
scholarrs17222919
googlers17222919
pharmgkbrs17222919
gwascentralrs17222919
openSNPrs17222919
23andMers17222919
23andMe allrs17222919
SNP Nexus

SNPshotrs17222919
SNPdbers17222919
MSV3drs17222919
GWAS Ctlgrs17222919
GMAF0.1607
Max Magnitude0

[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population


[PMID 20592751OA-icon.png] Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.


[PMID 25815512OA-icon.png] A Promoter Polymorphism (rs17222919, -1316T/G) of ALOX5AP Gene Is Associated with Decreased Risk of Ischemic Stroke in Two Independent Chinese Populations


[PMID 27416969] Genetic Variants in the Transcriptional Regulatory Region of the ALOX5AP gene and Susceptibility to Ischemic Stroke in Chinese Populations.